Allele/Variant

rs236482005

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:72222367

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)2:72222367C>T

HGVS.c name

ENSEMBL:ENSMUST00000090824.1:c.851+2447C>T
ENSEMBL:ENSMUST00000135469.1:c.851+2447C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:72115981...72272954 (156.97 kb)

Assembly version

Not Available

Viewer Help

Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

	Sequence feature	Sequence feature type	Associated gene	Location	Molecular consequence	Codon and amino acid change
	ENSEMBL:ENSMUST00000090824	protein_coding		Intron 10/19	intron variant
	ENSEMBL:ENSMUST00000135469	protein_coding		Intron 10/11	intron variant
	RefSeq:NM_001164791.2	protein_coding		Intron 10/11	intron variant
	RefSeq:NM_023057.6	protein_coding		Intron 10/19	intron variant
	RefSeq:XM_006499997.4	protein_coding		Intron 10/19	intron variant
	RefSeq:XM_006499998.4	protein_coding		Intron 1/10	intron variant
	RefSeq:XM_030251937.2	protein_coding		Intron 10/11	intron variant
	RefSeq:XR_004940679.1	transcript		Intron 10/11	intron variant

Showing 1 - 8 of 8 rows

per page

1